Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Ester type curable compound, composition containing same, cured product, and method for producing ester type curable compound

A manufacturing method and compound technology, which is applied in the field of ester-type curable compound manufacturing, can solve the problems that heat resistance and flexibility cannot be satisfied at the same time

Inactive Publication Date: 2014-04-30
小桧山登
View PDF8 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the current situation is that even with this method, heat resistance and flexibility cannot be satisfied at the same time.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Ester type curable compound, composition containing same, cured product, and method for producing ester type curable compound
  • Ester type curable compound, composition containing same, cured product, and method for producing ester type curable compound
  • Ester type curable compound, composition containing same, cured product, and method for producing ester type curable compound

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0102] Add 152 parts of tetrahydrophthalic anhydride, 74 parts of glycidol, 97 parts of diethylene glycol monoethyl ether acetate, and 0.226 parts of three Phenylphosphine was reacted at 70 to 80° C. for 6 hours to obtain a reaction solution containing a compound having an acid value of 167 mgKOH / g and an epoxy equivalent of 341 g / eq. It corresponds to n≈0.5 of the aforementioned general formula (1), that is, a mixture of compound (k1) and compound (k2). The infrared absorption spectrum (infrared absorption spectrometry (hereinafter referred to as "IR spectrum")) of the obtained compound is shown in figure 1 , the chromatogram obtained by gel permeation chromatography is shown in figure 2 . Then, add 202 parts of cresol novolac type epoxy resins (epoxy equivalent 202g / eq.), 190 parts of diethylene glycol monoethyl ether acetate, and 1.1 parts of triphenylphosphine in this reaction solution, at 90~ The reaction was carried out at 100° C. for 10 hours to obtain a reaction s...

Embodiment 2

[0115] 323.226 parts of the mixture solution of compound (k1) and compound (k2) obtained in Example 1, 47.7 parts of acrylic acid, 21 parts of diethylene diethylene glycol, Alcohol monoethyl ether acetate and 0.87 parts of triphenylphosphine were reacted at 90 to 100° C. for 8 hours while blowing air in, to obtain a reaction solution with 70% of non-volatile content. The acid value of the ester-type curable compound thus obtained was 197 mgKOH / g.

[0116] Then, 143 parts of the reaction solution obtained, 106 parts of cresol novolak type epoxy resin (epoxy equivalent 202g / eq.), 1 part of dicyandiamide, 25 parts of trimethylolpropane trimethacrylate, and 10 parts of 2-methyl-1-[4-(methylthio)phenyl]-2-morpholinopropan-1-one were kneaded to obtain a photo- and heat-curable composition. The composition is coated on a polyester film with a thickness of 50-60 μm, and the coating film is dried in a hot air circulation dryer at 80°C for 30 minutes, and then heated at 500mJ / cm 2 It ...

Embodiment 3

[0118] 392.796 parts and 76 parts of the ester-type curable compound solution obtained in Example 2 with 70% non-volatile components and an acid value of 197 mgKOH / g were added to a reaction container equipped with a thermometer, a stirrer, a reflux condenser tube, and an air blowing tube. A reaction in which diethylene glycol monoethyl ether acetate and 16.4 parts of 2,2'-azobisisobutyronitrile were reacted at 70-80°C for 8 hours while blowing nitrogen gas to obtain 60% of non-volatile components solution. The acid value of the ester-type curable compound thus obtained was 195 mgKOH / g, and Mw was 14,700. The IR spectrum of the obtained ester type curable compound is shown in Figure 4 .

[0119] Next, 167 parts of the obtained reaction solution, 105 parts of cresol novolak type epoxy resins (202 g / eq. of epoxy equivalent), and 1 part of dicyandiamide were kneaded, and the thermosetting composition was obtained. Then, it carried out similarly to Example 1, the test film and...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
acid valueaaaaaaaaaa
acid valueaaaaaaaaaa
epoxy equivalentaaaaaaaaaa
Login to View More

Abstract

An ester type curable compound which contains a structure represented by general formula (2), said structure being obtained using a compound that is represented by general formula (1). (In the formulae, G represents a glycidyl group; X represents a dibasic acid residue or a dibasic acid anhydride residue; R represents a glycidyl group or a hydrogen atom; and n represents an integer of 0 or more.)

Description

technical field [0001] The present invention relates to ester-type curable compounds used in various resists, adhesives, casting agents, laminated materials, paints, and sealants, compositions containing the same, cured products, and ester-type curable compounds. Manufacturing method. Background technique [0002] Epoxy resins represented by bisphenol A epoxy resins are currently widely used in adhesives, casting agents, lamination materials, coatings, and sealants due to their excellent heat resistance, adhesiveness, and chemical resistance. and other purposes. Regarding this epoxy resin, along with the recent development of the semiconductor industry, not only improvements in properties such as heat resistance, chemical resistance, and adhesiveness, but also flexibility are required, and new epoxy resins satisfying the above properties have been proposed. [0003] For example, a linear polynuclear epoxy compound containing different types of aromatic rings regularly and ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C08G59/00C08G63/91
CPCC08G63/91C08G59/00C08G59/42
Inventor 小桧山登
Owner 小桧山登
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com